Visitor Monitoring Drug Details: ELMIRON
 
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Drug Details

Drug Name: ELMIRON
FDA Application No: (NDA) 020193
Active Ingredient(s): PENTOSAN POLYSULFATE SODIUM
Company: ORTHO MCNEIL PHARM
Original Approval or Tentative Approval Date: September 26, 1996
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
O Orphan drug
 
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ELMIRON PENTOSAN POLYSULFATE SODIUM100MGCAPSULE; ORAL Prescription Yes None


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On Monday, September 2, 2013 Cherie Tate wrote:
 
Respond to a post that Jackie sent on August 25th. What do you mean by last post about will it cause. False or positive results on a 12 panel drug sreen. How would I find the 12 panel drug sceen to know what drugs are on the 12 panel drug screen?
On Sunday, August 25, 2013 Cherie Tate wrote:
 
I don't understand the reply from Jackie on Friday July 26, 2013. I didn't write until August 24, 2013.
On Saturday, August 24, 2013 Cherie Tate wrote:
 
I have been on elmiron 300mg a day for painful chronic interstial cystitis for 35 yrs. I tell lab persnonel that it can cause false psitives. As it says on cvs pamphlet. But it does not say for what. Most lab techs and doctor's do not know what it is. I take chronic pain mefsmeds opiates. Last drug tested positive fora opiate I don't take. Could it be the elmiron
On Friday, July 26, 2013 jackie wrote:
 
will it cause positive or false positive drug screen on a 12 panel drug test
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